Human Phenotype Ontology

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
Morphological abnormality of the nerves of the inner ear (HP:0011391)

Parent Node:
Abnormality of the vestibular nerve (HP:0011392)

..Starting node
..Hypoplasia of the vestibular nerve (HP:0011394)

Term ID:

11394

Name:

Hypoplasia of the vestibular nerve

Synonym:

Hypoplasia of cranial nerve VIII; Hypoplasia of the eighth cranial nerve; Thin vestibular nerve

Definition:

Underdevelopment of the vestibular nerve.

Comments:

Reference:

HP:0011394

Genes and Diseases:

Child Nodes:

Sister Nodes:

Aplasia of the vestibular nerve. (HP:0011393)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011394	HP:0011394	Hypoplasia of the vestibular nerve	0	CL E G H

Genes (0) :

Diseases (0) :

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.